Carbon fiber sizing agent, carbon fiber strand, and fiber-reinforced composite
a technology of carbon fiber strands and sizing agents, which is applied in the direction of fiber treatment, textiles and papermaking, transportation and packaging, etc., can solve the problems of deteriorating the properties of resultant fiber-reinforced composites, insufficient cohesion of reinforcement fiber strands, and inability to feed continuously chopped fiber to pellet manufacturing, etc., to achieve good bonding performance, excellent performance, and excellent properties
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examples
[0091]The present invention is specifically explained with the following examples, though the present invention is not restricted within the scope of the examples. The percent mentioned in the following examples means “wt % (weight percent)” unless otherwise specified. The properties were measured in the methods described below.
[Glass Transition Temperature]
[0092]The glass transition temperature of about 10 mg of a sample was determined with a differential scanning calorimeter (DSC, the Jade DSC Lab system, manufactured by PerkinElmer Instruments) according to JIS K 7121 with elevating temperature at the rate of 10 deg.C. / min. Specifically, a sample was accurately weighed to 10±1 mg and set in the differential scanning calorimeter, and the sample was heated under the elevating temperature up to the temperature 30 deg.C. higher than the melting temperature of the sample previously determined. Then the temperature of the sample was lowered to the temperature 50 deg.C. lower than the g...
example of production 1
[0102]In a reactor charged with nitrogen gas, 950 parts of dimethyl isophthalate, 1000 parts of diethylene glycol, 0.5 parts of zinc acetate and 0.5 parts of antimony trioxide were placed, and transesterification was conducted at a temperature ranging from 140 deg.C. to 220 deg.C. for 3 hours. Then 30 parts of sodium 5-sulfoisophthalate was added and esterification was conducted at a temperature ranging from 220 deg.C. to 260 deg.C. for 1 hour followed with condensation reaction under reduced pressure at a temperature ranging from 240 deg.C. to 270 deg.C. for 2 hours. The components of the resultant aromatic polyester resin determined in an analysis with NMR are as follows.
[0103]Isophthalic acid: 49 mol %
[0104]Diethylene glycol: 50 mol %
[0105]Sodium 5-sulfoisophthalate: 1 mol %
[0106]Then 200 parts of the resultant aromatic polyester resin and 100 parts of ethylene glycol monobutyl ether are placed in an emulsification device and agitated at a temperature ranging from 150 deg.C. to 1...
example of production 2
[0107]In a reactor charged with nitrogen gas, 760 parts of dimethyl terephthalate, 190 parts of dimethyl isophthalate, 750 parts of ethylene glycol, 250 parts of diethylene glycol, 0.5 parts of zinc acetate and 0.5 parts of antimony trioxide were placed, and transesterification was conducted at a temperature ranging from 140 deg.C. to 220 deg.C. for 3 hours. Then 30 parts of sodium 5-sulfoisophthalate was added and esterification was conducted at a temperature ranging from 220 deg.C. to 260 deg.C. for 1 hour followed with condensation reaction under reduced pressure at a temperature ranging from 240 deg.C. to 270 deg.C. for 2 hours. The components of the resultant aromatic polyester resin determined in an analysis with NMR are as follows.
[0108]Terephthalic acid: 39 mol %
[0109]Isophthalic acid: 10 mol %
[0110]Ethylene glycol: 40 mol %
[0111]Diethylene glycol: 10 mol %
[0112]Sodium 5-sulfoisophthalate: 1 mol %
[0113]Then 200 parts of the resultant aromatic polyester resin and 100 parts of...
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Abstract
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